Allele Registry

Canonical Allele Identifier: PA645374278

Gene: GRIN2B HGNC NCBI

ClinVar RCV:

RCV000223164

RCV001172341

ClinVar Variation:

234587

HGVS (amino-acid)	Matching Registered Transcripts
NP_000825.2:p.Lys976del	CA10577440 NM_000834.3:c.2926_2928del